Canonical Allele Identifier: CA2671517362
Gene: ADH1B HGNC NCBI

Linked Data

gnomAD v4: 4-99307892-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99307892T>C , CM000666.2:g.99307892T>C GRCh38
NC_000004.11:g.100229049T>C , CM000666.1:g.100229049T>C GRCh37
NC_000004.10:g.100448072T>C NCBI36
NG_011435.1:g.18524A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000305046.13:c.1104-28A>G MANE Select ENSP00000306606.8:n.1104-28A>G
ENST00000639454.1:c.1104-28A>G ENSP00000491622.1:n.1104-28A>G
ENST00000305046.12:c.1104-28A>G ENSP00000306606.8:n.1104-28A>G
ENST00000506651.5:c.984-28A>G ENSP00000425998.2:n.984-28A>G
ENST00000515694.4:n.3199-28A>G
ENST00000625860.2:c.984-28A>G ENSP00000486614.1:n.984-28A>G
NM_000668.5:c.1104-28A>G NP_000659.2:n.1104-28A>G
NM_001286650.1:c.984-28A>G NP_001273579.1:n.984-28A>G
NM_000668.6:c.1104-28A>G MANE Select NP_000659.2:n.1104-28A>G
NM_001286650.2:c.984-28A>G NP_001273579.1:n.984-28A>G
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